FDA Food recall F-0215-2014
EDGE, Item number 21-620, dietary supplement, 60 packet per box
- FDA Food
- Class I
- terminated
- Published 2013-11-27
On 2013-11-27 the FDA classified a Class I recall of EDGE, Item number 21-620, dietary supplement, 60 packet per box by New Algae, citing EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0215-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-10-23 |
| Published | 2013-11-27 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | New Algae |
| Distribution | US |
Product
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsules) per day. The suggested use for the "Before" packet is one packet (or 4 capsules) per day.
Reason
EDGE dietary supplement product is recalled because the finished label does not declare shark cartilage.
Identifiers
| code_info | Lot BO1 and AO1, Expiration date Aug 2015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0215-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.